Molecular mechanism of Xuebijing in treating pyogenic liver abscess complicated with sepsis.

IF 2.6 3区 医学 Q1 EMERGENCY MEDICINE World journal of emergency medicine Pub Date : 2024-01-01 DOI:10.5847/wjem.j.1920-8642.2024.016
Wei Zhou, Maiying Fan, Xiang Li, Fang Yu, En Zhou, Xiaotong Han
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Abstract

Background: Xuebijing (XBJ) can alleviate the inflammatory response, improve organ function, and shorten the intensive care unit (ICU) stay in patients with pyogenic liver abscess (PLA) complicated with sepsis, but the molecular mechanisms have not been elucidated. This study aimed to explore the molecular mechanism of XBJ in treating PLA complicated with sepsis using a network pharmacology approach.

Methods: The active ingredients and targets of XBJ were retrieved from the ETCM database. Potential targets related to PLA and sepsis were retrieved from the GeneCards, PharmGKB, DisGeNet, Online Mendelian Inheritance in Man (OMIM), Therapeutic Targets Database (TTD), and DrugBank databases. The targets of PLA complicated with sepsis were mapped to the targets of XBJ to identify potential treatment targets. Protein-protein interaction networks were analyzed using the STRING database. Potential treatment targets were imported into the Metascape platform for Gene Ontology (GO) functional enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses. Molecular docking was performed to validate the interactions between active ingredients and core targets.

Results: XBJ was found to have 54 potential treatment targets for PLA complicated with sepsis. Interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor (TNF) were identified as core targets. KEGG enrichment analysis revealed important pathways, including the interleukin-17 (IL-17) signaling pathway, the TNF signaling pathway, the nuclear factor-kappa B (NF-κB) signaling pathway, and the Toll-like receptor (TLR) signaling pathway. Molecular docking experiments indicated stable binding between XBJ active ingredients and core targets.

Conclusion: XBJ may exert therapeutic effects on PLA complicated with sepsis by modulating signaling pathways, such as the IL-17, TNF, NF-κB, and TLR pathways, and targeting IL-1β, IL-6, and TNF.

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雪碧净治疗化脓性肝脓肿并发败血症的分子机制
背景:雪碧(XBJ)可以减轻化脓性肝脓肿并发脓毒症患者的炎症反应,改善器官功能,缩短重症监护室(ICU)的住院时间,但其分子机制尚未阐明。本研究旨在利用网络药理学方法探讨XBJ治疗化脓性肝脓肿并发败血症的分子机制:方法:从ETCM数据库中检索XBJ的有效成分和靶点。从GeneCards、PharmGKB、DisGeNet、Online Mendelian Inheritance in Man (OMIM)、Therapeutic Targets Database (TTD)和DrugBank数据库中检索了与聚乳酸和败血症相关的潜在靶点。将脓毒症并发 PLA 的靶标与 XBJ 的靶标进行映射,以确定潜在的治疗靶标。使用 STRING 数据库分析了蛋白质-蛋白质相互作用网络。潜在的治疗靶点被导入Metascape平台进行基因本体(GO)功能富集和京都基因组百科全书(KEGG)通路富集分析。进行分子对接以验证活性成分与核心靶点之间的相互作用:结果:研究发现XBJ有54个潜在的治疗靶点,可用于治疗脓毒症并发聚乳酸。白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子(TNF)被确定为核心靶点。KEGG 富集分析揭示了重要的通路,包括白细胞介素-17(IL-17)信号通路、TNF 信号通路、核因子卡巴 B(NF-κB)信号通路和 Toll 样受体(TLR)信号通路。分子对接实验表明,XBJ 活性成分与核心靶点之间存在稳定的结合:XBJ可通过调节信号通路,如IL-17、TNF、NF-κB和TLR通路,以及靶向IL-1β、IL-6和TNF,对并发败血症的解放军发挥治疗作用。
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来源期刊
CiteScore
2.50
自引率
28.60%
发文量
671
期刊介绍: The journal will cover technical, clinical and bioengineering studies related to multidisciplinary specialties of emergency medicine, such as cardiopulmonary resuscitation, acute injury, out-of-hospital emergency medical service, intensive care, injury and disease prevention, disaster management, healthy policy and ethics, toxicology, and sudden illness, including cardiology, internal medicine, anesthesiology, orthopedics, and trauma care, and more. The journal also features basic science, special reports, case reports, board review questions, and more. Editorials and communications to the editor explore controversial issues and encourage further discussion by physicians dealing with emergency medicine.
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